What is MCADD: Symptoms, Causes and Treatment?

MCADD (medium-chain acyl-CoA dehydrogenase deficiency) is an inherited metabolic condition in which the body cannot properly break down certain fats for energy, particularly during periods without food, such as illness or missed meals. Without proper management, this can lead to a serious drop in blood sugar and, in severe cases, be life-threatening.

MCADD is identified through the newborn heel prick screening test, allowing preventive management to begin early. With appropriate care — mainly avoiding long periods without food, especially during illness — most children with MCADD develop normally and lead healthy lives.